Public Health Trace

Get Alerts

Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,341

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 2026

Most affected stateHawaii 200 recalls mention this state

State: GU ×
Clear all

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated October 28, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

EPINEPHrine 1:1000 INJECTION SOLUTION (PF) Syringe, 1 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0947-01

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

EDETATE DISODIUM 15% INJECTABLE, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0922-30

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

EDETATE CALCIUM DISODIUM 150MG/ML INJECTABLE, 100 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0934-11

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

DIMERCAPTO-PROPANESULFONIC 5% (DMPS)( (PFV) INJ SOL, 5 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0904-05

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

CYANCOBALAMIN 1200MCG/ML MDV INJECTION, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0946-30

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Copper 0.4MG/ML (PVF) INJECTION SOLUTION, 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0925-10

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

BUFFERED LIDOCAINE 1%+EPI 1:100,000 INJ SOL, [3ML NDC: 70731-0137-03 and 30ML NDC: 70731-0137-30] per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0137-03

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Ascorbic Acid 500 MG/ML (Non-Corn) INJ (MDV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0975-50

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution, 65 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0914-65

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 5, 2020Historical recordClass II

CVS Health Children's Nasal Saline Drops with Himalayan Salt Saline Nasal Moisturizer, 30 single-use vials per Carton,0.05 fl. oz. (1.5 mL) each 1.5 fl. oz. (45 mL) total, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, UPC 050428598207

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Mental Tonic Capsules, Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Thyro-Lo, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Stone Purger Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Migraine Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 13, 2023Historical recordClass II

Lump Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

Data last updated: October 28, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.